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Solitary orbital fibrous tumor in a 12-year-old child

机译:一个12岁的孩子的孤立眶纤维肿瘤

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Solitary orbital fibrous tumor was diagnosed in a 12-year old boy admitted to hospital for right-sided exophthalmos. MRI revealed orbital mass and surgical resection was performed. Histologically the tumor was composed of round or spindle cells with a lot of multinucleate giant cells and pseudovascular spaces. The neoplasm was regarded as a mixoid type of a solitary giant cell-rich fibrous tumor. Immunohistochemical analysis revealed coexpression of CD34, CD99, bcl-2, and CD99 (mic-2). The most important clinical, morphological, and immunohistochemical manifestations are presented in the paper. Major criteria for the differential diagnosis of solitary orbital fibrous tumor and the similar soft tissue tumors are discussed.
机译:孤立眶纤维肿瘤被诊断为一个12岁的男孩,入院右侧渗透滴漏。 MRI揭示了眶块和手术切除。 组织学上肿瘤由圆形或主轴细胞组成,具有许多多核巨细胞和假血管空间。 肿瘤被认为是富含纯细胞富含纤维瘤的混合型。 免疫组织化学分析显示CD34,CD99,BCL-2和CD99(MIC-2)的共表达。 本文提出了最重要的临床,形态和免疫组化表现。 讨论了孤立眶纤维肿瘤的差异诊断的主要标准和类似的软组织肿瘤。

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